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Protective Effects of an Oligo-Fucoidan-Based Formula against Osteoarthritis Development via iNOS and COX-2 Suppression following Monosodium Iodoacetate Injection.
Chiang, Yi-Fen; Huang, Ko-Chieh; Wang, Kai-Lee; Huang, Yun-Ju; Chen, Hsin-Yuan; Ali, Mohamed; Shieh, Tzong-Ming; Hsia, Shih-Min.
Afiliação
  • Chiang YF; School of Nutrition and Health Sciences, College of Nutrition, Taipei Medical University, Taipei 110301, Taiwan.
  • Huang KC; School of Nutrition and Health Sciences, College of Nutrition, Taipei Medical University, Taipei 110301, Taiwan.
  • Wang KL; Department of Nursing, Deh Yu College of Nursing and Health, Keelung 203301, Taiwan.
  • Huang YJ; Department of Biotechnology and Food Technology, Southern Taiwan University of Science and Technology, Tainan 710301, Taiwan.
  • Chen HY; School of Nutrition and Health Sciences, College of Nutrition, Taipei Medical University, Taipei 110301, Taiwan.
  • Ali M; Department of Obstetrics and Gynecology, University of Chicago, Chicago, IL 60637, USA.
  • Shieh TM; Clinical Pharmacy Department, Faculty of Pharmacy, Ain Shams University, Cairo 11566, Egypt.
  • Hsia SM; School of Dentistry, China Medical University, Taichung 404328, Taiwan.
Mar Drugs ; 22(5)2024 May 06.
Article em En | MEDLINE | ID: mdl-38786602
ABSTRACT
Osteoarthritis (OA) is a debilitating joint disorder characterized by cartilage degradation and chronic inflammation, accompanied by high oxidative stress. In this study, we utilized the monosodium iodoacetate (MIA)-induced OA model to investigate the efficacy of oligo-fucoidan-based formula (FF) intervention in mitigating OA progression. Through its capacity to alleviate joint bearing function and inflammation, improvements in cartilage integrity following oligo-fucoidan-based formula intervention were observed, highlighting its protective effects against cartilage degeneration and structural damage. Furthermore, the oligo-fucoidan-based formula modulated the p38 signaling pathway, along with downregulating cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression, contributing to its beneficial effects. Our study provides valuable insights into targeted interventions for OA management and calls for further clinical investigations to validate these preclinical findings and to explore the translational potential of an oligo-fucoidan-based formula in human OA patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoartrite / Polissacarídeos / Ciclo-Oxigenase 2 / Óxido Nítrico Sintase Tipo II Limite: Animals / Humans / Male Idioma: En Revista: Mar Drugs Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoartrite / Polissacarídeos / Ciclo-Oxigenase 2 / Óxido Nítrico Sintase Tipo II Limite: Animals / Humans / Male Idioma: En Revista: Mar Drugs Ano de publicação: 2024 Tipo de documento: Article